W140X_human-LIPA

General

Gene Locus : human-LIPA

Mode of mutation : Natural mutant

Disease : Wolman disease WD, Cholesterol Ester Storage Disease, CESD

Summary :

AAA Change :

Allelic Variant :

Risk Factor :

Inhibitor :

Structure :

Disease by interaction :

Interact Gene Locus :

Xenobiotic sensitivity :

Modification :

Torpedo_number : No torpedo number

Kinetic Parameter : No kinetic parameter

News : No news

Comment : p.Trp140Ter W140X c419G>A Homozygote with Wolman disease p.Trp119Ter W119X in mature protein. Found also as compound heterozygote with c894G>A, p.Ser275_GLn298del S275_Q298del Found also as compound heterozygote with c.851C>T (p.Ser284Phe)

References (4)

Title : Distinguishing Lysosomal Acid Lipase Deficiency From Familial Hypercholesterolemia - Sheth_2023_JACC.Case.Rep_24_102023
Author(s) : Sheth S , Toth PP , Baum SJ , Aggarwal M
Ref : JACC Case Rep , 24 :102023 , 2023
Abstract : Sheth_2023_JACC.Case.Rep_24_102023
ESTHER : Sheth_2023_JACC.Case.Rep_24_102023
PubMedSearch : Sheth_2023_JACC.Case.Rep_24_102023
PubMedID: 37869222

Title : A Novel Variant in the LIPA Gene Associated with Distinct Phenotype - Sarajlija_2022_Balkan.J.Med.Genet_25_93
Author(s) : Sarajlija A , Armengol L , Maver A , Kitic I , Prokic D , Cehic M , Djuricic MS , Peterlin B
Ref : Balkan Journal of Medical Genetics , 25 :93 , 2022
Abstract : Sarajlija_2022_Balkan.J.Med.Genet_25_93
ESTHER : Sarajlija_2022_Balkan.J.Med.Genet_25_93
PubMedSearch : Sarajlija_2022_Balkan.J.Med.Genet_25_93
PubMedID: 36880034
Gene_locus related to this paper: human-LIPA

Title : Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variants - Pisciotta_2017_Atherosclerosis_265_124
Author(s) : Pisciotta L , Tozzi G , Travaglini L , Taurisano R , Lucchi T , Indolfi G , Papadia F , Di Rocco M , D'Antiga L , Crock P , Vora K , Nightingale S , Michelakakis H , Garoufi A , Lykopoulou L , Bertolini S , Calandra S
Ref : Atherosclerosis , 265 :124 , 2017
Abstract : Pisciotta_2017_Atherosclerosis_265_124
ESTHER : Pisciotta_2017_Atherosclerosis_265_124
PubMedSearch : Pisciotta_2017_Atherosclerosis_265_124
PubMedID: 28881270
Gene_locus related to this paper: human-LIPA

Title : Lysosomal lipase deficiency: molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease - Fasano_2012_Mol.Genet.Metab_105_450
Author(s) : Fasano T , Pisciotta L , Bocchi L , Guardamagna O , Assandro P , Rabacchi C , Zanoni P , Filocamo M , Bertolini S , Calandra S
Ref : Mol Genet Metab , 105 :450 , 2012
Abstract : Fasano_2012_Mol.Genet.Metab_105_450
ESTHER : Fasano_2012_Mol.Genet.Metab_105_450
PubMedSearch : Fasano_2012_Mol.Genet.Metab_105_450
PubMedID: 22227072
Gene_locus related to this paper: human-LIPA